Devices

A chronically implanted macro-sieve electrode with large transit zones enabling robust axon regeneration and selective stimulation in a rat sciatic nerve transection model.

Device — Peripheral nerve

Macro-sieve regenerative electrode with transit zones (MacEwan et al., 2016)

PNI · regenerative · macro-sieve · transit zones · preclinical · stimulation · nerve transection · peripheral nerve

Macro-sieve regenerative electrode with transit zones (MacEwan et al., 2016)

One-line verdict: A regenerative sieve redesign that uses large “transit zones” (instead of dense micro-pores) to support healthier axon regeneration while enabling multi-site stimulation.

Quick tags: Regenerative interface · Stimulation · Species: rat · Status: preclinical


Overview

What it is: A polyimide-based macro-sieve electrode implanted between transected sciatic nerve stumps in a guidance conduit. Axons regenerate through several large transit zones; electrode sites surround the zones to stimulate the regenerated axons.

Why it matters: Dense micro-sieves can constrict/regulate axons in ways that harm caliber/myelination and limit functional recovery. Macro-scale transit zones are a design move to preserve axon health while still providing spatially separated electrode sites for selective stimulation.

Most comparable devices: micro-sieve electrodes, hyperflexible sieve meshes, microchannel scaffolds.


Spec Card Grid

Identity

  • Device name: Macro-sieve electrode (MSE)
  • Canonical ID: BTSD-PNI-0009-02
  • Key authors: MacEwan et al.
  • Org / manufacturer: academic research build
  • First demonstrated (year): 2016
  • Species: rat
  • Regulatory / trial status: preclinical
  • Primary use: regenerative stimulation interface
  • Primary target: transected sciatic nerve

Geometry & Architecture

  • Interface type: regenerative macro-sieve
  • Penetrating?: yes (regenerated axons pass through transit zones)
  • Transit zones: nine large zones reported (including a central zone and surrounding zones)
  • Substrate: polyimide (reported)
  • Anchoring / alignment: silicone conduit guidance between nerve stumps
  • Insertion method: nerve transection → MSE in conduit → proximal/distal alignment

Electrode & Channel Physics

  • Stimulation sites: eight metallized electrode sites reported (surrounding the transit zones)
  • Electrode material: Pt-Ir metallization is reported; electrode site surface treatment (e.g., Pt black) is reported in the paper
  • Recording modality: not primary; electrophysiology is assessed via evoked responses/distal measures
  • Stimulation capability: yes; monopolar stimulation through individual sites used to demonstrate selective muscle activation
  • Charge injection / safe stim range: build-specific; not standardized as a single number here

Tissue Interface & Bioresponse

  • Target tissue: regenerating axons
  • Design intent: preserve axon caliber/myelination vs micro-sieve constriction
  • Encapsulation: expected; chronic implantation context evaluated in the paper

System Architecture

  • Onboard electronics: none
  • Data path: wired external stimulation/recording in animal study

Performance Envelope

  • Regeneration: at ~3 months post-implant, fiber counts through MSE transit zones comparable to open conduit in the study
  • Function: stimulation of regenerated nerve through MSE evoked muscle forces comparable to open conduit; selective stimulation of individual muscles was demonstrated
  • Key limitation: requires nerve transection

Clinical / Preclinical Evidence

  • Model: rat sciatic nerve transection
  • Endpoints: histology + electrophysiology + muscle force outcomes
  • Key limitations: no human data; surgical transection requirement

Engineering Verdict

Strengths:

  • addresses axon constriction/health bottleneck for micro-sieves
  • demonstrates functional stimulation through regenerated nerve

Limitations / failure modes:

  • invasive (transection)
  • limited scaling without added routing/packaging complexity

References

  • MacEwan MR, et al. Regenerated Sciatic Nerve Axons Stimulated through a Chronically Implanted Macro-Sieve Electrode. Front Neurosci. 2016;10:557. doi: 10.3389/fnins.2016.00557. PubMed: https://pubmed.ncbi.nlm.nih.gov/28008303/